628316-36-9

Upstream product

• 106-02-5 pentadecanolide 
• 4356-77-8 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 404868-09-3 3,17-dihydroxy-heptadecanoic acid tert-butyl ester 
• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 
• 10548-46-6 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose 
• 404867-97-6 (3R)-tert-butyl [17-tert-butyldiphenylsilyloxy-3-(2,3,4-tri-O-benzyl-6-O-acetyl-β-D-glucopyranosyl)oxy]heptadecanoate 
• 404867-96-5 17-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-heptadecanoic acid tert-butyl ester 
• 125164-10-5 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 628316-35-8 (3R)-tert-butyl-[3-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-glucopyranosyl)oxy]heptadecanoate 

Downstream Products

• 628316-38-1 (3R,17S,23R)-3-((2R,3R,4S,5R,6R)-6-Acetoxymethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yloxy)-23-benzyloxy-17-hydroxy-tetracosanoic acid tert-butyl ester 
• 628316-39-2 (3R,17R,23R)-3-((2R,3R,4S,5R,6R)-6-Acetoxymethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yloxy)-23-benzyloxy-17-hydroxy-tetracosanoic acid tert-butyl ester 

Relevant academic research and scientific papers

Total Synthesis of Macroviracin D (BA-2836-4)

The first total synthesis of the complex glycolipid macroviracin D (BA-2836-4) (1) is described. This antivirally active metabolite isolated from the mycelium extracts of Streptomyces sp. BA-2836 incorporates a unique 46-membered macrodilactone motif deco

Structure Assignment, Total Synthesis, and Antiviral Evaluation of Cycloviracin B1

The first total synthesis of the antivirally active glycolipid cycloviracin B1 (1) is described. The approach is based on a two-directional synthesis strategy which constructs the C 2-symmetrical macrodiolide core of the target by an